chronic diarrhea Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of chronic diarrhea, which is usually taken to mean diarrhea that has persisted for over 4 weeks. (Human Phenotype Ontology, HP_0002028)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002028
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Genes

16 genes associated with the chronic diarrhea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATP7A ATPase, Cu++ transporting, alpha polypeptide
CASP8 caspase 8, apoptosis-related cysteine peptidase
COG4 component of oligomeric golgi complex 4
COG6 component of oligomeric golgi complex 6
CR2 complement component (3d/Epstein Barr virus) receptor 2
ETHE1 ethylmalonic encephalopathy 1
HEXB hexosaminidase B (beta polypeptide)
IKBKB inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase beta
IL21 interleukin 21
IL21R interleukin 21 receptor
IL2RA interleukin 2 receptor, alpha
IL2RG interleukin 2 receptor, gamma
ITCH itchy E3 ubiquitin protein ligase
LRBA LPS-responsive vesicle trafficking, beach and anchor containing
SLC10A2 solute carrier family 10 (sodium/bile acid cotransporter), member 2
SLC5A1 solute carrier family 5 (sodium/glucose cotransporter), member 1